2-chloroethane-(thiono)-phosphonic acid amido esters

ABSTRACT

CERTAIN NOVEL 2-CHLOROETHANE-(THIONO)-PHOSPHONIC ACID AMIDO COMPOUNDS OF THE FORMULA   CL-CH2-CH2-P(=X)(-Y-R&#39;&#39;)-NH-R   IN WHICH X AND Y WHICH MAY BE THE SAME OF DIFFERENT ARE OXYGEN OR SULFUR, R IS HYDROGEN OR ALKYL, AND R&#39;&#39; IS ALKYL OR IF R IS HYDROGEN OR Y IS SULFUR R&#39;&#39; MAY ADDITIONALLY BE PHENYL WHICH MAY BE SUBSTITUTED BY HYDROXY, (LOWER) ALKYL, HALOGEN OR NITRO. POSSESS MARKED PLANT GROWTH REGULANT PROPERTIES, E.G. SELECTIVE HERBICIDAL ACTIVITY, GROWTH PROMOTING AND GROWTH ALTERING PROPERTIES.

United States Patent 3,825,635 Z-CHLOROETHANE-(THION0)-PHOSPHONIC ACID AMIDO ESTERS Wolfgang Hofer, Wuppertal-Vohwinkel, Reinhard Schliebs, Cologne, Robert Schmidt, Leverkusen, and Ludwig Eue, Cologne, Germany, assignors to Bayer Aktiengesellschaft, Leverkusen, Germany No Drawing. Filed Mar. 1, 1971, Ser. No. 119,912 Claims priority, application Germany, Mar. 4, 1970, P 20 119.3 Int. Cl. C07f 9/40, 9/42, 9/44 US. Cl. 260-959 17 Claims ABSTRACT OF THE DISCLOSURE Certain novel 'il-chloroethane-(thiono)-phosphonic acid amido compounds of the formula C1-CH:CHz-l NH-R in which X and Y, which may be the same or different, are oxygen or sulfur, R is hydrogen or alkyl, and R is alkyl, or, if R is hydrogen or Y is sulfur, R may additionally be phenyl which may be substituted by hydroxy, (lower) alkyl, halogen or nitro.

possess marked plant growth regulant properties, e.g., selective herbicidal activity, growth promoting and growth altering properties.

The present invention relates to certain novel 2-chloroethane-(thiono)-phosphonic acid amido compounds, to plant growth regulant compositions containing them, and to their use as plant growth regulating agents.

It is known from Netherlands Patent Specification 6802633 that Z-chloroethanephosphonic acid exhibits plant-growth-regulating properties.

Surprisingly, it has now been found that certain 2- chloroethane-(thiono)-phosphonic acid amido compounds according to the invention show a notably greater plantgrowth-regulating activity than the 2-chloroethanephosphonic acid known from the prior art, which may be regarded as the structurally closest art compound having the same type of activity. The substances according to the invention therefore represent a valuable enrichment of the art.

The compounds of present invention are 2-chloroethane-(thiono)-phosphonic acid amido compounds of the general formula YR (I) in which X and Y, which may be the same or different, are oxygen or sulfur,

R is hydrogen or alkyl, e.g., lower alkyl, and

R is alkyl, e.g., lower alkyl, or, if R is hydrogen or Y is sulfur, R may additionally be phenyl which may be substituted by hydroxy, (lower) alkyl, halogen or nitro.

R is preferably hydrogen or alkyl with 1 to 4 carbon atoms. R is preferably alkyl with 1 to 4 carbon atoms or a phenyl radical substituted by nitro, methyl, hydroxy and/ or chlorine.

These compounds exhibit strong plant-growth-regulating properties.

3,825,635 Patented July 23, 1974 The present invention also provides a process for the production of a 2-chloroethane-(thiono)-phosphonic acid amido compound of the formula (I) in which (a) a 2-chloroethanethiono)-phosphonic acid amide chloride of the general formula 10 in which X has the meaning stated above and R" is alkyl,

preferably with 1 to 4 carbon atoms,

is reacted with a compound of the general formula x ClCHr-CHz-l Hal R (IV) in which X, Y and R have the meaning stated above, and Hal is halogen (preferably chlorine or bromine), is reacted with a compound of the general formula in which R has the meaning stated above,

optionally in the presence of an acid-binding agent and optionally in the presence of a solvent.

If 2-chloroethanephosphonic acid N-monomethylamide chloride and p-chlorothiophenol are used as starting materials, the reaction course according to process variant (a) can be represented by the following formula scheme:

If 2-chloroethanethionophosphonic acid phenyl ester chloride and ammonia are used as starting materials, the reaction course according to process variant (b) can be represented by the following formula scheme:

CI--CH2CHr-i'-NH' The starting materials are defined generally by the formulae (II) to (V).

As examples of the amines of the formula (V), alcohols, mercaptans, phenols and thiophenols of the formula (III), there are mentioned in particular:

ammonia, methyl, ethyl, propyl and n-, sec.-, lerL- or isobutyl amine,

methanol, ethanol, propanol and 11-, sec.-, tert.- or isobutyl alcohol,

methyl, ethyl, propyl, iso-propyl and butyl mercaptan, 2-, 3- and 4-chlorophenol, 2-, 3- and 4-nitrophenol, 2-, 3- and 4-methylphenol as well as resorcinol, catechol and hydroquinone, thiophenol, m-, p-thiocresol and 2- and 4-chlorothiophenol.

The amines, alcohols, mercaptans, phenols and thiophenols used as starting materials are known and can be prepared according to known methods.

The 2-chloroethane-(thiono)-phosphonic acid ester chlorides or amido chlorides of the formulae (IV) or (II), respectively, used as starting materials are not known but can be obtained in simple manner according to known methods by reaction of 2-chloroethane-(thiono)-phosphonic acid dichloride with amines, alcohols, mercaptans phenols or thiophenols (the phenols and thiophenols possibly being used in the form of their alkali metal salts, alkaline earth metal salts or ammonium salts), optionally in the presence of an acid-binding agent and optionally, in the presence of a solvent, at temperatures from to +50 C.

Examples (a) to (d) set forth below illustrate this process:

Example aPreparation of 2-chloroethanethionophosphonic acid N-monomethyl amide chloride S N HCH:

15.5 g. (0.5 mole) methylamine in 200 ml. toluene are added to 49.5 g. (0.25 mole) 2-chloroethanethionophosphonic acid dichloride in 500 ml. toluene. Stirring was afterwards effected for one hour at room temperature; the salts were then filtered off with suction, washing with water and drying over sodium sulfate are efiected, and the solvent was drawn olf. After slight distillation at 0.01 mm. Hg/80 C., a yellow oil remained behind. Yield: 41 g. (85%) 2-chloroethanethionophosphonic acid N- monomethyl amide chloride, n =-1.56l3.

Analysis:

Calculated for C H CI NPS: S 16.65%, N 7.30% Found: S 16.47%, N 7.35%

Example b--Preparation of 2-chloroethanethionophosphonic acid phenyl ester chloride 19 g. (0.2 mole) phenol in 50 ml. H 0 and 8 g. (0.2 mole) sodium hydroxide are added to 39.5 g. (0.2 mole) 2-chloroethanethionophosphonic acid dichloride at 20 C. Stirring for 2 hours at room temperature was afterwards effected, followed by taking up in methylene chlo ride, separation of the organic phase and washing with water. After drying over sodium sulfate had been carried out, the solvent was drawn olf and slight distillation (1 mm. Hg/60" C.) was then effected. Yield: 39 g. (77%) 2-chloroethanethionophosphonic acid phenyl ester chloride as colourless liquid, n =1.5688.

Analysis:

Calculated for C H CI OPS: S 12.55%, Cl 27.90% Found: S 12.46%, Cl 28.82%

Example c-Preparation of 2-chloroethanephosphonic acid N-monoisopropylamide chloride 59 g. (1 mole) iso-propylamine are added to 91 g. (0.5 mole) 2-chloroethanephosphonic acid dichloride in 1.5 l. of toluene at 0 C. Stirring was afterwards effected for one hour at room temperature, the salts were filtered off with suction, the solution was Washed with a little water and the solvent was drawn off with suction; slight distillation was then effected (0.01 mm. Hg/ C.). Yield: 93 g. (91%) 2-chloroethanephosphonic acid 'N- monoisopropylamide chloride; n =1.4854.

Analysis:

Calculated for C H Cl NOP: N 6.85%, Cl 34.80% Found: N 6.58%, Cl 33.74%

Example (1 Analogously with Example c, there is prepared 2-chloroethane-phosphonic acid N-mono-methylamide chloride 0 NH-CH:

Yield: 56%, n =1.50l9.

To obtain the compounds of the present invention, as indicated above, either process variant according to the present invention may be carried out in the presence of a solvent (this term includes a mere diluent). The solvent may for example be water or an inert organic solvent. Such solvents include aliphatic and aromatic (possibly chlorinated) hydrocarbons such as benzene, toluene, xylene, benzine, methylene chloride, chloroform, carbon tetrachloride, chlorobenzene; ethers, such as diethyl ether, dibutyl ether, dioxan; ketones, such as acetone, methylethyl ketone, methylisopropyl ketone, methylisobutyl ketone; and nitriles, such as acetonitrile.

An acid-binding agent may be used, as mentioned above. All customary acid-binding agents are suitable. Particularly suitable are alkali metal carbonates and alcoholates, such as sodium and potassium carbonate and sodium and potassium methylate or ethylate; and aliphatic, aromatic or heterocyclic amines, such as triethy1- amine, dimethylaniline, dimethylbenzylamine and pyridine.

The reaction temperatures can be varied within a fairly wide range. In general, the work is carried out at from -20 to C., preferably 0 to 60.

The reactions are generally carried out at normal pressure.

When carrying out the process variants according to the invention, approximately 1 mole of alcohol, mercaptan, phenol or thiophenol and approximately 1 mole of acid acceptor used per mole of (thiono) phosphonic acid amide chloride; approximately 2 moles of primary amine or ammonia are used per mole of (thiono) phosphonic acid ester chloride. The reactions may be carried out in water or another suitable solvent, in most cases at room temperature. A slight excess of the compounds of formulae (III) and (IV) is not detrimental.

Working up may take place according to customary methods. The substances according to the invention are obtained in most cases in the form of colourless to slightly yellow-coloured, viscous, water-insoluble oils which cannot be distilled without decomposition but can, by so-called slight distillation (that is, by longer heating to moderately elevated temperatures under vacuum), be freed from the last volatile components and can in this way 'be purifled. For their characterization, the refractive index is especially useful. If the compounds are obtained in crystalline form, the melting point serves for their characterization.

The following examples are illustrative: Example 1Preparation of 2-chloroethanephosphonic acid isopropyl ester N-monoisopropylamide 24 g. (0.4 mole) isopropanol and 33 g. (0.33 mole) triethylamine are added to 67 g. (0.33 mole) 2-chloroethanephosphonic acid N-monoisopropylamide chloride in 200 ml. benzene at room temperature. Stirring was afterwards effected for 2 hours at 50 0., followed by suction filtration from precipitated salt, and the reaction solution was washed with water. After drying with sodium sulfate and drawing off the solvent, slight distillation was effected. There remained behind a colourless oil, n =1.4686, yield: 50 g. (67%) 2-chloroethanephosphonic acid isopropyl ester N-monoisopropylamide.

Analysis:

Calculated for C H CINO P: 15.65% C1,6.15% N Found: 16.05% Cl, 6.36% N The 2-chloroethane-phosphonic acid N-mono-isopropylamide chloride used as starting product was prepared from 2-chloroethane-phosphonic acid dichloride and iso-propylamine in toluene at 0 C. Yield: 91% of the theory, n =l.4854.

Example 2-Preparation of 2-chloroethanephosphonic acid ethyl ester N-monoisopropylamide 87 ml. (0.2 mole) ethanolic sodium ethylate solution are added to 41 g. (0.2 mole) 2-chloroethanephosphonic acid N-monoisopropylamide chloride in 200 ml. benzene at room temperature. Stirring was afterwards effected for 2 hours; the salts were then filtered off with suction, the reaction solution was washed with water, and drying with sodium sulfate was effected. After the solvent had been drawn off, slight distillation was carried out. There remained behind a colourless oil, n =1.4580, yield: 27 g. (64%) 2-chloroethanephosphonic acid ethyl ester N- monoisopropylamide.

Analysis:

Calculated for C'IHNCINOZPZ 16.65% Cl, 6.60% N Found: 16.33% Cl, 6.56% N Starting product compare Example 1.

Example 3-Preparation of 2-chloroethanethiophosphonic acid S-ethyl ester N-monoisopropylamide 13 g. (0.2 mole) ethyl mercaptan and 20 g. (0.2 mole) triethylamine are added to 41 g. (0.2 mole) 2-chloroethanephosphonic acid N-rnonoisopropylamide chloride in 100 ml. benzene. Stirring was afterwards effected for 2 hours at 40 C.; the salts were then filtered oif with suction, the reaction solution was washed with Water, and drying with sodium sulfate was carried out. After the solvent had been drawn off, there remained behind a crystalline residue, m.p. 51 0, yield: 15 g. (33%) 2-chloroethanethiophosphonic acid S-ethyl ester N-monoisopropylamide.

Analysis:

Calculated for C H ClNOPS: 15.45% Cl, 6.10% N,

13.95% S Found: 15.30% C], 6.08% N, 13.80% S Starting product compare Example 1.

Example 4 Preparation of 2-chloroethane-thio-phosphonic acid S- phenyl ester N-monoisopropylamide was prepared analogously with Example 3, m.p. 61 C., yield: 59% 2-chloroethane-thio-phosphonic acid S-phenyl ester N-monoisopropylamide.

Analysis:

Calculated for C H ClNOPS: 5.50% N, 11.50% S Found: 5.55% N, 11.95% S Example 5-Preparation of 2 chloroethanethionophosphonic acid phenyl ester amide Cl-OHrCHz-iPi-NH:

Analysis:

Calculated for C H CINOPS: 15.05% Cl, 5.95% N,

12.60% S Found: 14.82% Cl, 5.21% N, 12.42% S The starting product used was prepared from 2-chloroethanethiono-phosphonic acid dichloride and sodium phenolate in water, n =1.568S', yield: 77% 2-chloroethanethionophosphonic acid phenyl ester chloride.

Example 6--Preparation of 2-ch'loroethanethionophosphonic acid -4-chlorophenyl ester amide 87 g. (0.3 mole) 2-chloroethanethionophosphonic acid 4'-chlorophenyl ester chloride in 500 ml. benzene are treated with gaseous ammonia at room temperature until the solution was saturated with ammonia. Stirring was afterwards effected for one hour; the salt was then filtered off with suction, and the reaction solution was washed with water. After drying with sodium sulfate, the solvent was drawn off. After slight distillation, there remained behind a colourless oil, n =1.5945, yield: 62 g. (76%) 2- chloroethanethionophosphonic acid 4'-chlorophenyl ester amide.

Analysis:

Calculated for C H Cl NOPS: 26.15% Cl, 5.17%

N, 11.85% S Found: 26.23% Cl, 4.83% N, 11.65% S The starting product was prepared analogously with the starting product of Example 5, n =l.585 6, yield: 59% 2-chloroethane-thiono-phosphonic acid 4-chloro-phenyl ester chloride.

Example 7 Preparation of 2-chloroethane-thiono-phosphonic acid 2,4-dichloro-phenyl ester amide was prepared analogously with Example 6, n =1.6020, yield: 86%.

Analysis:

Calculated for C H Cl NOPS: 35.00% Cl, 10.5% Found: 35.54% Cl, 10.1% S

The starting product was prepared analogously with the starting product of Example 5, n =1.5962, yield: 60% 2-chloroethane-thiono-phosphonic acid 2,4-dichlorophenyl ester chloride.

The Z-chloroethane (thiono) phosphonic acid derivatives of this invention interfere with the physiological phenomena of plant growth and can therefore be used as plant growth regulators.

The diiferent eifects of these active compounds depend essentially on the point in time of the application, with reference to the development stage of the seed or the plant, as well as on the concentrations applied.

Plant growth regulators are used for various purposes which are connected with the development stage of the plants. Thus, with plant growth regulators the seed germination can either be inhibited or promoted, depending on the concentration applied. This inhibition or promotion relates to the seedling development.

The bud dormancy of the plants, that is to say the endogenic annual cycle, can be influenced by the active compounds, so that the plants may for example shoot or blossom at a point in time at which they normally show no readiness to shoot or blossom.

The shoot or root growth can be promoted or inhibited by the active compounds in manner dependent on concentration. Thus, it is possible for example to inhibit very strongly the growth of the fully formed plant, or to bring the plant as a whole to a more robust habitus or to produce a dwarf growth.

An example of an economic application is the suppression of grass growth at roadsides and waysides. Further, the growth of lawns can be inhibited by growth regulators, so that the frequency of grass-cutting (of lawn-mowing) can be reduced.

During the growth of the plant, the branching to the side can be multiplied by a chemical breaking of the apical dominance. This can be a valuable feature for example in the case of propagation of plants by cuttings. In concentration-dependent manner, however, it is also possible to inhibit the growth of side-shoots, for example in tobacco plants in order to prevent the formation of sideshoots after decapitation and thus to promote the leaf growth.

In the case of the influencing of blossom formation, there can be achieved, in manner dependent on concentration and the time of the application, either a retarding or an acceleration of blossom formation. Under certain circumstances, a multiplication of blossom initiation can be attained, these effects occurring when the appropriate treatments are carried out at the time of the normal blossom formation.

The influence of the active compound on the foliage of the plants can be so regulated that a defoliation is achieved, for example in order to facilitate the harvest or to reduce transpiration at a time at which plants are to be transplanted.

Fruit initiation can be promoted so that more, or seedless, fruits are formed (parthenocarpy). Under certain conditions, the premature fall of fruit can also be prevented, or the fruit fall can be promoted up to a certain extent in the sense of a chemical thinning out. The promotion of the fruit fall can, however, also be so exploited that the treatment is effected at the time of the harvest, whereby harvesting is facilitated.

By spraying unripe fruits with the compounds according to the invention, the ripening process can be accelerated and a better colouring of the fruits can be achieved.

The active compounds according to the present invention can be converted into the usual formulations, such as solutions, emulsions, suspension, powders, pastes and granulates. These may be produced in known manner, for example by mixing the active compounds with extenders, that is, liquid or solid diluents or carriers, optionally with the use of surface-active agents, that is, emulsifying agents and/ or dispersing agents. In the case of the use of water as an extender, organic solvents can, for example, also be used as auxiliary solvents.

As liquid diluents or carriers, there are preferably used aromatic hydrocarbons, such as xylenes or benzene, chlorinated aromatic hydrocarbons, such as chlorobenzenes, paraffins, such as mineral oil fractions, alcohols, such as methanol or butanol, or strongly polar solvents, such as dimethyl formamide or dimethyl sulfoxide, as well as water.

As solid diluents or carriers, there are preferably used ground natural minerals, such as kaolins, clays, talc or chalk, or ground synthetic minerals, such as highly-dispersed silicic acid or silicates.

Preferred examples of emulsifying agents include nonionic and anionic emulsifiers, such as polyoxyethylenefatty acid esters, polyoxyethylene-fatty alcohol ethers, for example alkylarylpolyglycol ethers, alkyl sulfonates and aryl sulfonates; and preferred examples of dispersing aglents include lignin, sulfite waste liquors and methyl celu ose.

The formulations contain, in general, from 0.1 to 95, preferably 0.5 to 90, percent by weights of active compound.

The active compounds may be applied as such or in the form of their formulations or of the application forms prepared therefrom, such as ready-to-use solutions, emulsifiable concentrates, emulsions, suspensions, spray powders, pastes, soluble powders, dusting agents and granulates. Application may take place in the usual manner, for example by watering, squirting, spraying, scattering, dusting, etc.

The concentrations of active compound can be varied within a fairly wide range for actual application. In general, concentrations of 0.0005 to 2% by weight, preferably from 0.01 to 0.5%, are used.

There are applied, in general, 0.1 to -kg., preferably 1 to 10 kg., of active compound per hectare of soil area.

As regards the application time, there is generally a preferred space of time for application, depending on the object to be achieved, and on the climatic and vegetative circumstances.

The growth influencing characteristics of the compounds of this invention are illustrated by the following Examples.

10 compound. After 6 days, the average length and the The following compounds were tested:

Compound No. Structure Chemical name 1 NHC;H iso 2-chloroethanethiophosphonic acid-S-ethy1 ester N-monoisopropylamide. C1--CHr-CHz-P S -C 2H5 2 0 NHC H iso Z-ehloroethanethiophosphonic acld-S-phenyl ester N-monoisopropylamide. (ll-CHr-CHr-P 3 S NH; 2-chloroethanethionophosphonic acid-O- ll (4-ch1orophenyl)-ester amide. C1-CH2-CHz-P\ 4 O NH--C H1-iso 2-ehloroethanephosphonic acid isopropyl ester N -monoisopropylamide.

EXAMPLE A Growth inhibition/linseeds Solvent: 40 parts by weight acetone Emulsifier: 0.25 part by weight alkylaryl polyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound was mixed with the stated amount of solvent which contained the stated amount of emulsifier, and the concentrate was diluted with a disodium hydrogen phosphate-potassium dihydrogen phosphate buifer solution (pH 6) to the desired concentration.

Batches of 25 linseeds are laid out on 2 filter papers in a Petri dish. 10 ml. of the preparation of active compound are pipetted into each dish. Germination of the seeds takes place in the dark at C.

After three days, the length of the shoot was determined and the growth inhibition compared with the control plant was expressed as a percentage. 100% denotes the standstill of growth, and 0% denotes a growth corresponding to that of the untreated plant.

The active compounds, the concentration of the active compound in p.p.m. (=mg./kg.) and results can be seen from Table A.

Growth inhibition and defoliation/beans Solvent: parts by weight acetone Emulsifier: 0.25 part by weight alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound was mixed with the stated amount of solvent which contained the stated amount of emulsifier, and the concentrate was diluted with a disodium hydrogen phosphate-potassium dihydrogen phosphate buffer solution (pH 6) to the desired concentration.

Beans (Phaseolus vulgarz's) 10 cm. high are sprayed with preparations which contain 5000 ppm. of active number of leaves of 3 beans per experiment were evaluated.

The results can be seen from Table B.

TABLE B Growth inhibition and defoliation/beans Length in em. Number of leaves With 5,000 ppm.

Active compound Growth inhibition/tomato plants Solvent: 40 parts by weight acetone Emulsifier: 0.25 part by weight alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound was mixed with the stated amount of solvent which contained the stated amount of emulsifier, and the concentrate was diluted with a disodium hydrogen phosphate-potassium dihydrogen phosphate bufier solution (pH 6) to the desired concentration.

Tomato plants of a height of 10 cm. were sprayed with a preparation which contained 500 ppm. of active compound.

After 8 days, the percentage inhibition of the treated plants compared with the untreated control plant was determined. With inhibition, no growth was present; with 0% inhibition, the growth corresponds to that of the control plant.

The active compounds, concentration of active compound in ppm. (=mg./kg.) and the results can be seen from Table C.

1 1 EXAMPLE D Growth inhibition/ apple seedlings Solvent: 40 parts by weight acetone Emulsifier: 0.25 part by weight alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound was mixed with the stated amount of solvent which contained the stated amount of emulsifier, and the concentrate was diluted with a disodium hydrogen phosphate-potassium dihydrogen phosphate buffer solution (pH 6) to the desired concentration.

Apple seedlings are, at a height of about 2 cm., sprayed with a preparation which contains 500 p.p.m. of active compound. After 7 days, the percentage inhibition of the treated plants compared with the untreated control plant was determined. With 100% inhibition, no growth was present; with inhibition, the growth corresponds to that of the control plant.

Growth inhibition/Cynosurus Solvent: 40 parts by weight acetone Emulsifier: 0.25 part by weight alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound was mixed with the stated amount of solvent which contained the stated amount of emulsifier, and the concentrate was diluted with a disodium hydrogen phosphate-potassium dihydrogen phosphate buffer solution (pH 6) to the desired concentration.

A grass planting (Cyanosurus cristatus) was sprayed with a preparation (which contained 1000 p.p.m. of active compound) in an applied amount of 25 kg./ hectare. After 14 days, the retardation of grass growth was determined and expressed in compared with the untreated control.

The results can be seen from Table E.

TABLE E Growth inhibition/cynosurus Acceleration of fruit ripeness/ tomato plants Solvent: 40 parts by weight acetone Emulsifier: 0.25 part by weight alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound was mixed with the stated amount of solvent which contained the stated amount of emulsifier, and the concentrate was diluted with a disodium hydrogen phosphate-potassium dihydro- 12 gen phosphate buffer solution (pH 6) to the desired concentration.

Green, unripe fruits of tomato plants were sprayed once with a preparation which contained 5000 p.p.m. of active compound. An accelerated ripening of the fruits was thereby achieved.

The result can be seen from Table F.

It will be seen from the above description that the invention, in one aspect, provides a plant growth regulating composition containing as active ingredient a compound according to the invention in admixture with a solid diluent or carrier containing a surface-active agent.

The invention also provides a method of regulating plant growth which comprises applying to a plant a compound according to the invention alone or in the form of a composition according to the invention in admixture with a solid or liquid diluent or carrier.

It will be understood that the specification and examples are illustrative but not limitative of the present invention and that other embodiments with the spirit and scope of the invention will suggest themselves to those skilled in the art.

What is claimed is:

1. 2 Chloroethane-(thiono)-phosphonic acid amino compounds of the general formula in which X and Y, which may be the same or ditferent, are oxygen or sulfur,

R is hydrogen or lower alkyl, and R is lower alkyl, or, if R is hydrogen or Y is sulfur,

R' may additionally be phenyl which may be substituted by hydroxy, lower alkyl, halogen or nitro.

2. 2-Chloroethanephosph0nic acid amido compounds as claimed in claim 1.

3. 2-Chloroethane thionophosphonic acid amido com pounds as claimed in claim 1.

4. Compounds as claimed in claim 1 wherein R hydrogen.

5. Compounds as claimed in claim 1 wherein R alkyl of from 1 to 4 carbon atoms.

6. Compounds as claimed in claim 1 wherein R alkyl of from 1 to 4 carbon atoms.

7. Compounds as claimed in claim 1 wherein R is substituted phenyl wherein each substituent is selected from the group consisting of nitro, methyl, hydroxy and chloro.

8. Compounds as claimed in claim 1 wherein both X and Y are sulfur.

9. Compounds as claimed in claim 1 wherein both X and Y are oxygen.

10. Compounds as claimed in claim 1 wherein one of X and Y is sulfur and the other oxygen.

11. Compound as claimed in claim 1 designated 2- chloroethanephosphonic acid isopropyl ester N-monoiso-= propylamide.

12. Compound as claimed in claim 1 designated 2- chloroethanephosphonic acid ethyl ester N-monoisopropylamide.

13. Compound as claimed in claim 1 designated 2- chloroethanethiophosphonic acid Sethyl ester N-monoisopropylamide. .1

14. Compound as claimed in claim 1 designated 2- cbloroethane-thio-phosphonic acid S-phenyl ester N- monoisopropyl amide.

15. Compound as claimed in claim 1 designated 2- chloroethanetlj ionophospl onic acid phenyl ester amide.

16. Compound as claimed in claim 1 designated 2- chloroethanethionophosphonic acid 4'-chl0rdphenyl ester amide. 1

17. Compound as claimed in claim 1 designated 2- chloroethane-thiono-phosphonic acid 2 ',4'-dichlorophenyl ester amide.

14 References Cited UNITED STATES PATENTS 3,679,780 7/ 1972 Randall et al. 260-959 3,644,600 2/1972 Beriger 260-959 3,010,986 11/ 1961 Reetz 260-959 X 3,185,721 5/ 1965 Schrader 260-959 X FOREIGN PATENTS 197,581 4/1967 U.S.S.R. 260-959 189,642 11/ 1964 U.S. S.R. 260-959 179,317 11/1964 U.S.S.R. 260-959 5 us. c1. xx. 71-86, 81; 260-953, 954, 912, 91:, m 

